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<br />4 <br /> <br />counts presented in Table 1 show agreement with other <br />data by the various authors. Vertebral counts reported <br />by Holden and Stalnaker (1970) did not include the <br />Weberian complex (four vertebrae), thus when four is <br />added to the counts presented in their Table 2 the range <br />in the count becomes 46-49 which is inclusive in our <br />counts (45-49) presented in Table 1. <br />In addition to the above counts we counted the prin- <br />cipal caudal rays and contrary to the count of 20 given <br />by Miller (1946) for the holotype, we found that 95 of <br />the 96 specimens had 19 caudal rays. The one atypical <br />count was 18. <br />The lateral line scale count was difficult to make on <br />some specimens, but even on those specimens the accu- <br />racy is within plus or minus two scales. Many specimens <br />had undulations in the lateral line row of scales, particu- <br />larly in the anterior portion. On a few specimens the <br />lateral line row had displaced sections of one to several <br />scales. <br />Pharyngeal arches were removed from twenty speci- <br />mens to determine nature of dentition. Miller (1946) <br />gave the dental formula of the holotype as 2,5 - 4,l? He <br />said there may have been a second tooth in the minor <br />row on the right arch. Seventeen of the twenty specimens <br />we examined have the typical Gila dental formula of <br />2,5 - 4,2. One specimen has 2,5 - 4,1, another specimen <br />has 1,5 - 4,2, and the remaining specimen of the twenty <br />examined has 2,5 - 5,2. The extra tooth on the right <br />arch is somewhat medial and practically has a common <br />base with the upper tooth of the major row. There is a <br />possibility that the two specimens with the single tooth <br />in the minor row on the one side did have two teeth and <br />one was broken off without leaving a trace of a stump <br />or a socket. However, the count may be correct in that <br />some specimens have very slender, delicate teeth in the <br />minor row and it is conceivable that this may be an in- <br />dication of a reduction in number. <br />X-rays of the larger specimens revealed a two-cham- <br />bered swim bladder. <br />A review of the 24 scattergrams (Figures 1 - 8) of pro- <br />portional measurements indicates a linear relationship <br />of all proportions with the standard length. Some obser- <br />vations do not appear on the scattergrams because of <br />overlap, but all data for each proportion were used to <br />compute regression formulae. <br /> <br />Sexual Dimorphism <br /> <br />Some males have decidedly longer pectoral and pelvic <br />fins than most females; however, a few females have <br />rather long paired fins. The relative position, size and <br />shape of the tubular termination of the digestive tract <br />(outlined with ink on illustrations) and the urogenital <br />papilla are quite different in the female and the male. <br />Figure 18 illustrates the anal region of an adult female, <br />and Figure 19 illustrates that of an adult male. The <br />tubular ending of the digestive tract of the female is long <br />and extended posteriorly (overlapping base of first anal <br />fin ray) so that the urogenital papilla is hidden under- <br /> <br />TULANE UNIVERSITY MUSEUM NATURAL HISTORY <br /> <br />neath when viewing the ventral surface of the fish. In <br />the male the terminal tube of the digestive tract is not <br />nearly so long and the urogenital papilla (indicated by <br />arrow on illustration) projects ventrally so that its tip is <br />visible just beyond the termination of the digestive tract. <br />Tuberculation of males and females differ consider- <br />ably. The nuptial male has larger tubercles and more <br />areas of the fins and body are studded with tubercles <br />than on the nuptial female. One of the four adult speci- <br />mens (TU 97918) collected from the mouth of Little <br />Colorado River during June of 1976 has small breeding <br />tubercles scattered over the top of the head, laterally to <br />the rim of the orbit and about half way ventrally on the <br />opercle. There is a progressively decreasing number of <br />tubercles on the hump from the nape toward the origin <br />of the dorsal fin. Tubercles extend nearly two-thirds the <br />distance toward the dorsal fin. There are no tubercles <br />on the underside of head, about the lips nor below the <br />orbit on the snout or cheek. Although the anteromedial <br />patches of scales in front of the bases of the pectoral fins <br />(breast patches) are developed with free posterior mar- <br />gins, there are none with developed tubercular ridges. <br />There are small tubercles developed on the upper surface <br />of the second, third and fourth pectoral fin rays and also <br />on the upper surface of the second, third, fourth and <br />fifth pelvic rays. We consider the above male fish to rep- <br />resent an early stage of nuptial development. <br />The salvage specimens (TU 100542) obtained from <br />Powell Reservoir were near spawning condition if not <br />actually spawning at the time of capture. The larger <br />specimen (Figure 17 lower) is a female (320 mm SL) <br />and the smaller (Figure 17 upper) a male (298 mm SL) . <br />Unfortunately we did not obtain the specimens until a <br />number of months after they had been captured on 5 <br />June 1975. The specimens exhibited some breeding color <br />even after having been frozen and stored in a freezer. <br />The entire lower side below dark pigmentation of the <br />body of the male was orange. The bases of pectoral and <br />anal fins were orange. The cheek below the eye was <br />yellowish and the iris was pinkish-orange. The female <br />was light orange on the lower portion of the side and at <br />the base of the anal fin. The base of the pectoral fin <br />was cream color. These colors may have been brighter <br />at the time of capture. <br />The tubercles and thickened epidermal layer had <br />sloughed off various parts of the body of these two speci- <br />mens during the delay in getting the specimens from the <br />field to the freezer and then subsequent freezing and <br />thawing. However, sufficient tuberculation remains to <br />allow a description of the sexual dimorphism in this <br />character. The male has rather large tubercles scattered <br />over the entire head (Figures 20 and 21) and smaller <br />ones p~steriorly on the hump to about two-thirds the <br />distance toward the origin of the dorsal fin. The thick- <br />ened epidermal layer is missing from part of this region, <br />and perhaps, tubercles were present all the way to the <br />dorsal fin. These predorsal tubercles are not particularly <br />associated with the embedded scales but are scattered <br />over the surface. Some tubercles occur over the scales <br />